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Merck
CN

126292

3,5-二甲氧基苯甲醛

98%

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线性分子式:
(CH3O)2C6H3CHO
化学文摘社编号:
分子量:
166.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-772-6
Beilstein/REAXYS Number:
2042374
MDL number:
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产品名称

3,5-二甲氧基苯甲醛, 98%

InChI key

VFZRZRDOXPRTSC-UHFFFAOYSA-N

InChI

1S/C9H10O3/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-6H,1-2H3

SMILES string

[H]C(=O)c1cc(OC)cc(OC)c1

assay

98%

form

solid

bp

151 °C/16 mmHg (lit.)

mp

45-48 °C (lit.)

functional group

aldehyde

Quality Level

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Application

常用作合成砌块。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

>233.6 °F

flash_point_c

> 112 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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A new poly(ethylene glycol)-modified DAT2-Cu(OAc)2 complex smoothly catalyzes a base-free nitroaldol condensation in a highly enantioselective manner (ee up to 93%) also in reagent-grade solvent and in the presence of air. Effective recovery and recycling (up to five runs) of
Katie A Keaton et al.
Organic letters, 9(14), 2717-2719 (2007-06-15)
A strategy for ketone synthesis with cyclopropanols as intermediates and its application to (+)-spirolaxine methyl ether is described. The synthesis also features an application of Fu's alkyl-alkyl Suzuki coupling.
Monika Osińska-Jaroszuk et al.
Bioprocess and biosystems engineering, 41(7), 973-989 (2018-03-28)
Four bacterial EPSs extracted from Rhizobium leguminosarum bv. trifolii Rt24.2, Sinorhizobium meliloti Rm1021, Bradyrhizobium japonicum USDA110, and Bradyrhizobium elkanii USDA76 were determined towards their metal ion adsorption properties and possible modification of Cerrena unicolor laccase properties. The highest magnesium and
Khuzaimah Arifin et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 120, 208-215 (2013-11-05)
A new homoleptic dithiolene tungsten complex, tris-{1,2-bis(3,5-dimethoxyphenyl)-1,2-ethylenodithiolene-S,S'}tungsten, was successfully synthesized via a reaction of the thiophosphate ester and sodium tungstate. The thiophosphate ester was prepared from 3,5-dimethoxybenzaldehyde via benzoin condensation to produce the intermediate 1,2-bis-(3,5-dimethoxyphenyl)-2-hydroxy-ethanone compound, followed by a reaction

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